Sonova Group
At Sonova, we envision a world where everyone can enjoy the delight of hearing. This vision inspires us and fuels our commitment to developing innovative solutions that improve hearing health and human connection - from personal audio devices and wireless communication systems to hearing aids and cochlear implants. We're dedicated to providing outstanding customer experiences through our global audiological care services, ensuring that everyone has the opportunity to engage fully with the world around them.
Guided by a culture of continuous improvement that fosters resilience and self-motivation, our team is united by a shared commitment to excellence and a deep sense of pride in our work, each of us playing a vital role in creating meaningful change.
Here you’ll find a diverse range of opportunities that span both consumer and medical solutions and the freedom to shape your career while making an impact on the lives of others. Join us in our mission to create a more connected world, where every voice is heard and every story matters.
Clinical Data Operations Manager Responsible for overseeing the collection, analysis, and interpretation of clinical data to support regulatory submissions, post‑market surveillance, and evidence generation. This role ensures data integrity, compliance with global regulatory standards (e.g., FDA, MDR, ISO 14155), and alignment with clinical research objectives. Additionally, the position collaborates with cross‑functional teams, including clinical operations, regulatory affairs, and biostatistics, to translate complex clinical data into actionable insights that drive product development, market adoption, and patient safety.
Responsibilities
Develop, maintain, and enforce standard operating procedures (SOPs) and work instructions for clinical data management.
Design, develop, and manage clinical study databases in compliance with FDA regulations, Quality System Regulations (QSR), and Good Clinical Practices (GCP).
Maintain clinical study hardware and software to support study execution.
Data Integrity & Reporting.
Develop reporting strategies for interim and final clinical data analysis.
Establish reporting frameworks to monitor operational study performance and ensure data consistency across studies.
Work closely with Clinical Operations to align data management strategies with overall trial execution.
Provide guidance and mentorship to in‑house and remote Clinical Data Management staff.
Foster a collaborative team environment and provide leadership to support high‑quality data collection and analysis.
Build and maintain effective working relationships with other group companies in Sonova, including providing support and guidance with respect to global clinical data operations.
Participate in resource forecasting and implement process improvements to enhance data management efficiency.
Stay current with industry trends and evolving regulatory requirements to ensure best practices.
Support other Clinical Research Department functions as needed to achieve department goals.
Other duties as assigned by your manager.
Travel Requirement Up to 20%.
Qualifications
Bachelor’s Degree in a related field (e.g., Life Sciences, Data Science, Clinical Research).
Extensive experience (5‑7 years) in clinical data management, particularly in an FDA‑regulated environment (Sponsor or Clinical Research Organization).
Strong knowledge of electronic data capture (EDC) systems, clinical database development, and regulatory compliance.
Prior experience working with international regulatory frameworks (e.g., EMA, PMDA, Health Canada) preferred.
Prior exposure to medical device trials and post‑market clinical follow‑up (PMCF) studies.
Hands‑on experience with advanced EDC and CTMS systems (e.g., Medidata Rave, Oracle Inform, Veeva).
Understanding of risk‑based monitoring (RBM) and centralized statistical monitoring.
Strong project management and organizational skills, with the ability to manage multiple initiatives simultaneously.
Ability to analyze engagement data and make data‑driven decisions to enhance employee experience.
Certification in Clinical Data Management, Project Management (PMP, PRINCE2), or Clinical Research (ACRP, SOCRA) preferred.
Experience with report development using MS‑SQL, MS Access & any procedure or object‑oriented programming languages desirable.
Familiarity with data visualization and analytics tools (e.g., Power BI, Tableau, Python, R).
A minimum of 200 Mb/sec download and 10 Mb/sec upload speed internet connectivity is required to support any remote/hybrid employee functionality at Sonova.
Benefits
Medical, dental and vision coverage*
Health Savings, Health Reimbursement, Flexible Spending/Dependent Care Accounts
TeleHealth options
401k plan with company match*
Company paid life/ad&d insurance
Additional supplemental life/ad&d coverage available
Company paid Short/Long‑Term Disability coverage (STD/LTD)
STD LTD buy‑ups available
Accident/Hospital Indemnity coverage
Legal/ID Theft Assistance
PTO (or sick and vacation time), floating Diversity Day, & paid holidays*
Paid parental bonding leave
Employee Assistance Program (24/7 mental health support hotline, 5 company paid counseling sessions and more)
Robust Internal Career Growth opportunities
Hearing aid discount for employees and family
Internal social recognition platform
This role's pay range is between $94,400/yr – $141,600/yr (compensation is based on skillset and location). This role is also bonus eligible.
How we work At Sonova, we prioritize the well‑being of our employees and foster an inclusive environment that promotes engagement and collaboration. Our team‑customized hybrid work model empowers teams to balance individual needs with business goals, offering flexibility and individualized time management. We recognize the importance of life outside of work and strive to create a supportive and motivating workplace where innovation thrives.
Equal Opportunity Employer We team up. We grow talent. We collaborate with people of diverse backgrounds to win with the best team in the marketplace. We guarantee every person equal treatment in regard to employment and opportunity for employment, regardless of a candidate’s ethnic or national origin, religion, sexual orientation or marital status, gender, genetic identity, age, disability or any other legally protected status.
#J-18808-Ljbffr
Guided by a culture of continuous improvement that fosters resilience and self-motivation, our team is united by a shared commitment to excellence and a deep sense of pride in our work, each of us playing a vital role in creating meaningful change.
Here you’ll find a diverse range of opportunities that span both consumer and medical solutions and the freedom to shape your career while making an impact on the lives of others. Join us in our mission to create a more connected world, where every voice is heard and every story matters.
Clinical Data Operations Manager Responsible for overseeing the collection, analysis, and interpretation of clinical data to support regulatory submissions, post‑market surveillance, and evidence generation. This role ensures data integrity, compliance with global regulatory standards (e.g., FDA, MDR, ISO 14155), and alignment with clinical research objectives. Additionally, the position collaborates with cross‑functional teams, including clinical operations, regulatory affairs, and biostatistics, to translate complex clinical data into actionable insights that drive product development, market adoption, and patient safety.
Responsibilities
Develop, maintain, and enforce standard operating procedures (SOPs) and work instructions for clinical data management.
Design, develop, and manage clinical study databases in compliance with FDA regulations, Quality System Regulations (QSR), and Good Clinical Practices (GCP).
Maintain clinical study hardware and software to support study execution.
Data Integrity & Reporting.
Develop reporting strategies for interim and final clinical data analysis.
Establish reporting frameworks to monitor operational study performance and ensure data consistency across studies.
Work closely with Clinical Operations to align data management strategies with overall trial execution.
Provide guidance and mentorship to in‑house and remote Clinical Data Management staff.
Foster a collaborative team environment and provide leadership to support high‑quality data collection and analysis.
Build and maintain effective working relationships with other group companies in Sonova, including providing support and guidance with respect to global clinical data operations.
Participate in resource forecasting and implement process improvements to enhance data management efficiency.
Stay current with industry trends and evolving regulatory requirements to ensure best practices.
Support other Clinical Research Department functions as needed to achieve department goals.
Other duties as assigned by your manager.
Travel Requirement Up to 20%.
Qualifications
Bachelor’s Degree in a related field (e.g., Life Sciences, Data Science, Clinical Research).
Extensive experience (5‑7 years) in clinical data management, particularly in an FDA‑regulated environment (Sponsor or Clinical Research Organization).
Strong knowledge of electronic data capture (EDC) systems, clinical database development, and regulatory compliance.
Prior experience working with international regulatory frameworks (e.g., EMA, PMDA, Health Canada) preferred.
Prior exposure to medical device trials and post‑market clinical follow‑up (PMCF) studies.
Hands‑on experience with advanced EDC and CTMS systems (e.g., Medidata Rave, Oracle Inform, Veeva).
Understanding of risk‑based monitoring (RBM) and centralized statistical monitoring.
Strong project management and organizational skills, with the ability to manage multiple initiatives simultaneously.
Ability to analyze engagement data and make data‑driven decisions to enhance employee experience.
Certification in Clinical Data Management, Project Management (PMP, PRINCE2), or Clinical Research (ACRP, SOCRA) preferred.
Experience with report development using MS‑SQL, MS Access & any procedure or object‑oriented programming languages desirable.
Familiarity with data visualization and analytics tools (e.g., Power BI, Tableau, Python, R).
A minimum of 200 Mb/sec download and 10 Mb/sec upload speed internet connectivity is required to support any remote/hybrid employee functionality at Sonova.
Benefits
Medical, dental and vision coverage*
Health Savings, Health Reimbursement, Flexible Spending/Dependent Care Accounts
TeleHealth options
401k plan with company match*
Company paid life/ad&d insurance
Additional supplemental life/ad&d coverage available
Company paid Short/Long‑Term Disability coverage (STD/LTD)
STD LTD buy‑ups available
Accident/Hospital Indemnity coverage
Legal/ID Theft Assistance
PTO (or sick and vacation time), floating Diversity Day, & paid holidays*
Paid parental bonding leave
Employee Assistance Program (24/7 mental health support hotline, 5 company paid counseling sessions and more)
Robust Internal Career Growth opportunities
Hearing aid discount for employees and family
Internal social recognition platform
This role's pay range is between $94,400/yr – $141,600/yr (compensation is based on skillset and location). This role is also bonus eligible.
How we work At Sonova, we prioritize the well‑being of our employees and foster an inclusive environment that promotes engagement and collaboration. Our team‑customized hybrid work model empowers teams to balance individual needs with business goals, offering flexibility and individualized time management. We recognize the importance of life outside of work and strive to create a supportive and motivating workplace where innovation thrives.
Equal Opportunity Employer We team up. We grow talent. We collaborate with people of diverse backgrounds to win with the best team in the marketplace. We guarantee every person equal treatment in regard to employment and opportunity for employment, regardless of a candidate’s ethnic or national origin, religion, sexual orientation or marital status, gender, genetic identity, age, disability or any other legally protected status.
#J-18808-Ljbffr